MEF35 - Plant Editosome Database - CNCB-NGDC

Summary

Editing Factor: MEF35
Synonym: MITOCHONDRIAL EDITING FACTOR 35
Description: The MEF35 protein contains eleven PPR repeats and E and DYW extensions at the C-terminus; Two T-DNA insertion mutants, one inserted just upstream and the other inside the reading frame encoding the DYW domain, show loss of editing at a site in each of the mRNAs for protein 16 in the large ribosomal subunit (site rpl16-209), for cytochrome b (cob-286) and for subunit 4 of complex I (nad4-1373), respectively; Editing is restored upon introduction of the wild type MEF35 gene in the reading frame mutant; Homozygous mutant plants develop indistinguishably from wild type plants, although the RPL16 and COB/CYTB proteins are essential and the amino acids encoded after the editing events are conserved in most plant species
Protein Family: Pentatricopeptide repeat (PPR) protein
Subclass: DYW
Physical Interaction: MORF1; MORF8
Construct Structure: PLS-E-E+-DYW
Gene ID & Species: AT4G14050 (Arabidopsis thaliana)
Edited Gene(s): rpl16    nad4    cob
Editing Type(s): C-to-U (21)
Publication(s): [1] Multiple PPR Protein Interactions Are Involved in the RNA Editing System in Arabidopsis Mitochondria and Plastids, Proc Natl Acad Sci U S A, 2017. [doi:10.1073/pnas.1705815114]
[2] The DYW Subgroup PPR Protein MEF35 Targets RNA Editing Sites in the Mitochondrial rpl16, nad4 and cob mRNAs in Arabidopsis thaliana, PLOS One, 2015. [doi:10.1371/journal.pone.0140680]

Editing Details

Species Gene ID Organelle Edited Gene Position Region Nuclear Genome Organelle Genome Other Region Other Position Editing Type Codon Amino Acid Molecular Effect Experiment Details
Arabidopsis thaliana AT4G14050 Mitochondrion cob 286 CDS NA NA NA NA C-to-U CUU=>UUU
NA=>NA
L=>F
NA=>NA
Recoding
NA
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
Col-0Col-0ControlControlNo mutantNormalNANADirect Sequencing of PCR Products100.00%CompleteNone26470017
SAIL_101_B01mef35-1T-DNA InsertionT-DNA is inserted in the upstreamHomozygousThe plants of mutant line mef35-1 show developmental and adult phenotypes indistinguishable from the WTNANADirect Sequencing of PCR Products0.00%UneditedAbsent26470017
SALK_060464mef35-2T-DNA InsertionT-DNA is inserted in the reading frame encoding the DYW domainHomozygousSeedlings of mutant line mef35-2 initially develop a little slower in comparison to the WT col plantlets, but look similar at the flowering stageNANADirect Sequencing of PCR Products0.00%UneditedAbsent26470017
SALK_060464mef35-2+MEF35ComplementationThe MEF35 NT (wt) Col reading frame is transformed under control of the 35S promoter in vector Pmdc123HomozygousRetarded growthNANADirect Sequencing of PCR ProductsNAHighRestored26470017
Col-0WTControlControlNo mutantNormalLeafNART-PCR and calculated with the DNADynamo software (BlueTract100.00%CompleteNone28761003
Col-0DYW2-GFP-OE1Generating Arabidopsis plants overexpressing the GFP-tagged DYW2 geneCol-0 A. thaliana plants were transformed with the 35S::DYW2-GFP plasmids (in pK7WGF2 backbone) by the floral-dip method. Transformed plants were selected based on Kanamycin resistance. Two independenNASlow growthLeafNART-PCR and calculated with the DNADynamo software (BlueTract100.00%CompleteSimilar28761003
Col-0DYW2-GFP-OE2Generating Arabidopsis plants overexpressing the GFP-tagged DYW2 geneCol-0 A. thaliana plants were transformed with the 35S::DYW2-GFP plasmids (in pK7WGF2 backbone) by the floral-dip method. Transformed plants were selected based on Kanamycin resistance. Two independenNASlow growthLeafNART-PCR and calculated with the DNADynamo software (BlueTract100.00%CompleteSimilar28761003
Arabidopsis thaliana AT4G14050 Mitochondrion nad4 1373 CDS NA NA NA NA C-to-U UCC=>UUC
NA=>NA
S=>F
NA=>NA
Recoding
NA
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
Col-0Col-0ControlControlNo mutantNormalNANADirect Sequencing of PCR Products100.00%CompleteNone26470017
SAIL_101_B01mef35-1T-DNA InsertionT-DNA is inserted in the upstreamHomozygousThe plants of mutant line mef35-1 show developmental and adult phenotypes indistinguishable from the WTNANADirect Sequencing of PCR Products0.00%UneditedAbsent26470017
SALK_060464mef35-2T-DNA InsertionT-DNA is inserted in the reading frame encoding the DYW domainHomozygousSeedlings of mutant line mef35-2 initially develop a little slower in comparison to the WT col plantlets, but look similar at the flowering stageNANADirect Sequencing of PCR Products0.00%UneditedAbsent26470017
SALK_060464mef35-2+MEF35ComplementationThe MEF35 NT (wt) Col reading frame is transformed under control of the 35S promoter in vector Pmdc123HomozygousRetarded growthNANADirect Sequencing of PCR ProductsNAHighRestored26470017
Col-0WTControlControlNo mutantNormalLeafNART-PCR and calculated with the DNADynamo software (BlueTract100.00%CompleteNone28761003
Col-0DYW2-GFP-OE1Generating Arabidopsis plants overexpressing the GFP-tagged DYW2 geneCol-0 A. thaliana plants were transformed with the 35S::DYW2-GFP plasmids (in pK7WGF2 backbone) by the floral-dip method. Transformed plants were selected based on Kanamycin resistance. Two independenNASlow growthLeafNART-PCR and calculated with the DNADynamo software (BlueTract100.00%CompleteSimilar28761003
Col-0DYW2-GFP-OE2Generating Arabidopsis plants overexpressing the GFP-tagged DYW2 geneCol-0 A. thaliana plants were transformed with the 35S::DYW2-GFP plasmids (in pK7WGF2 backbone) by the floral-dip method. Transformed plants were selected based on Kanamycin resistance. Two independenNASlow growthLeafNART-PCR and calculated with the DNADynamo software (BlueTract95.00%HighSimilar28761003
Arabidopsis thaliana AT4G14050 Mitochondrion rpl16 209 CDS NA NA NA NA C-to-U ACU=>AUU
NA=>NA
T=>I
NA=>NA
Recoding
NA
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
Col-0Col-0ControlControlNo mutantNormalNANADirect Sequencing of PCR Products100.00%CompleteNone26470017
SAIL_101_B01mef35-1T-DNA InsertionT-DNA is inserted in the upstreamHomozygousThe plants of mutant line mef35-1 show developmental and adult phenotypes indistinguishable from the WTNANADirect Sequencing of PCR Products0.00%UneditedAbsent26470017
SALK_060464mef35-2T-DNA InsertionT-DNA is inserted in the reading frame encoding the DYW domainHomozygousSeedlings of mutant line mef35-2 initially develop a little slower in comparison to the WT col plantlets, but look similar at the flowering stageNANADirect Sequencing of PCR Products0.00%UneditedAbsent26470017
SALK_060464mef35-2+MEF35ComplementationThe MEF35 NT (wt) Col reading frame is transformed under control of the 35S promoter in vector Pmdc123HomozygousRetarded growthNANADirect Sequencing of PCR ProductsNAHighRestored26470017
Col-0WTControlControlNo mutantNormalLeafNART-PCR and calculated with the DNADynamo software (BlueTract96.00%HighNone28761003
Col-0DYW2-GFP-OE1Generating Arabidopsis plants overexpressing the GFP-tagged DYW2 geneCol-0 A. thaliana plants were transformed with the 35S::DYW2-GFP plasmids (in pK7WGF2 backbone) by the floral-dip method. Transformed plants were selected based on Kanamycin resistance. Two independenNASlow growthLeafNART-PCR and calculated with the DNADynamo software (BlueTract100.00%CompleteSimilar28761003
Col-0DYW2-GFP-OE2Generating Arabidopsis plants overexpressing the GFP-tagged DYW2 geneCol-0 A. thaliana plants were transformed with the 35S::DYW2-GFP plasmids (in pK7WGF2 backbone) by the floral-dip method. Transformed plants were selected based on Kanamycin resistance. Two independenNASlow growthLeafNART-PCR and calculated with the DNADynamo software (BlueTract100.00%CompleteSimilar28761003
Last update: Sep 2026 (version 2.0)